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Rare disease
Explore subjects recorded in this category. Classifications come from Wikidata and have not been independently checked here.
Appearing here does not make a subject a governed Counterpedia record. Data and provenance
21
Subjects
21
Recorded classifications
0
Partial type records
Members
- Waardenburg's syndrome
Source identity
Provider: Wikidata · Entity ID: Q1151801 - syndactyly
Source identity
Provider: Wikidata · Entity ID: Q1360044 - focal segmental glomerulosclerosis
Source identity
Provider: Wikidata · Entity ID: Q1435223 - Kabuki syndrome
Source identity
Provider: Wikidata · Entity ID: Q1538227 - erythropoietic protoporphyria
Source identity
Provider: Wikidata · Entity ID: Q1759600 - thanatophoric dysplasia
Source identity
Provider: Wikidata · Entity ID: Q1787020 - Pelizaeus-Merzbacher disease
Source identity
Provider: Wikidata · Entity ID: Q1876206 - moya moya disease
Source identity
Provider: Wikidata · Entity ID: Q1951267 - hypoparathyroidism-deafness-renal disease syndrome
Source identity
Provider: Wikidata · Entity ID: Q2027515 - Paget's disease of bone
Source identity
Provider: Wikidata · Entity ID: Q2035074 - Marfan syndrome
Source identity
Provider: Wikidata · Entity ID: Q208562 - X-linked adrenal hypoplasia congenita
Source identity
Provider: Wikidata · Entity ID: Q3144300 - achromatopsia
Source identity
Provider: Wikidata · Entity ID: Q432396 - hereditary spastic paraplegia 23
Source identity
Provider: Wikidata · Entity ID: Q4664694 - phaeochromocytoma
Source identity
Provider: Wikidata · Entity ID: Q536269 - multiple endocrine neoplasia type 2A
Source identity
Provider: Wikidata · Entity ID: Q604075 - Apert syndrome
Source identity
Provider: Wikidata · Entity ID: Q618246 - metabolic syndrome
Source identity
Provider: Wikidata · Entity ID: Q657193 - osteitis fibrosa cystica
Source identity
Provider: Wikidata · Entity ID: Q799615 - Barth syndrome
Source identity
Provider: Wikidata · Entity ID: Q928424 - primary polydipsia
Source identity
Provider: Wikidata · Entity ID: Q929963
End of this category
Data and provenance
Provider: Wikidata · Category ID: Q929833. Recorded label: rare disease. Membership uses exact P31 (“instance of”) statements, without inferred or subclass membership.
21 statement rows; 30327 bounded bytes read. This technical read limit does not assess source support.
- Public release
- sha256:f33228901a35b0683356002a46df9ceb11f399d05f17abb5c7c78256cbf38ba7
- Projection source release
- sha256:ea0e40d1cd430ab2f1d2f7ea45cdc3ab22f0bbbf772a96703a721cbe8ea97843
- Membership artifact
- sha256:fe67438914b44adac201a6f2e1418c785c89b6fed9968462d434c31e35c7c628
- Class artifact
- sha256:4cbcdf13236398a2f13c6da6b53a520cf6a4a5ed42eea9845cf5579e08995ef8
- Class index
- sha256:a1b2f7c2f9c519553c259832c7130d876c684487a7f759f252e4974e67032f41
- Source adjacency
- sha256:9e459e3e17aa2f90f5bab367d26abbe50a97f1d9a775566ff425beab9f3170d0
These identifiers make the carried projection inspectable and reproducible. They are provenance bindings, not truth, support, admission, verification, or authority claims.